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Oligosaccharide solid-phase synthesis cleavage conditions

Solid-phase Oligosaccharide Synthesis. Methanesulfonyl chloride resin 1 was used as an activating linker in the synthesis of various polymer-bound di and trisaccharides 2 (eq 1). The sulfonate linker proved stable to glycosidation and alcohol deprotection conditions, and nucleophilic displacement of 2 by Nal provided 6-iodosaccharides (eq 1). NaOAc and NaNs were also suitable nucleophiles for cleavage of the sulfonate linker. ... [Pg.545]

See other pages where Oligosaccharide solid-phase synthesis cleavage conditions is mentioned: [Pg.11] [Pg.79] [Pg.105] [Pg.137] [Pg.321] [Pg.41] [Pg.383] [Pg.490] [Pg.101] [Pg.4] [Pg.69] [Pg.113] [Pg.224] [Pg.229] [Pg.263]

See also in sourсe #XX -- [ Pg.241 , Pg.247 ]

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Oligosaccharides solid-phase synthesis

Solid oligosaccharides

Solid-phase synthesi